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2022

This folder holds the following references to publications, sorted by year and author.

There are 4 references in this bibliography folder.

Aldisi, R, Hassanin, E, Sivalingam, S, Buness, A, Klinkhammer, H, Mayr, A, Fröhlich, H, Krawitz, P, and Maj, C (2022).
GenRisk: a tool for comprehensive genetic risk modeling
Bioinformatics:btac152.

Coutelier, M, Holtgrewe, M, Jäger, M, Flöttman, R, Mensah, MA, Spielmann, M, Krawitz, P, Horn, D, Beule, D, and Mundlos, S (2022).
Combining callers improves the detection of copy number variants from whole-genome sequencing
European Journal of Human Genetics, 30(2):178--186.

Hsieh, T, Bar-Haim, A, Moosa, S, Ehmke, N, Gripp, KW, Pantel, JT, Danyel, M, Mensah, MA, Horn, D, Rosnev, S, Fleischer, N, Bonini, G, Hustinx, A, Schmid, A, Knaus, A, Javanmardi, B, Klinkhammer, H, Lesmann, H, Sivalingam, S, Kamphans, T, Meiswinkel, W, Ebstein, F, Krüger, E, Küry, S, Bézieau, S, Schmidt, A, Peters, S, Engels, H, Mangold, E, Kreiß, M, Cremer, K, Perne, C, Betz, RC, Bender, T, Grundmann-Hauser, K, Haack, TB, Wagner, M, Brunet, T, Bentzen, HB, Averdunk, L, Coetzer, KC, Lyon, GJ, Spielmann, M, Schaaf, CP, Mundlos, S, Nöthen, MM, and Krawitz, PM (2022).
GestaltMatcher facilitates rare disease matching using facial phenotype descriptors
Nature Genetics.

Uellendahl-Werth, F, Maj, C, Borisov, O, Juzenas, S, Wacker, EM, Jørgensen, IF, Steiert, TA, Bej, S, Krawitz, P, Hoffmann, P, Schramm, C, Wolkenhauer, O, Banasik, K, Brunak, S, Schreiber, S, Karlsen, TH, Degenhardt, F, Nöthen, M, Franke, A, Folseraas, T, and Ellinghaus, D (2022).
Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease
Communications Biology, 5(1):80.

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